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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376631Generated: November 2, 2026

Aminoisobutyric acid → HCID 22916684, compound

https://huagongshe.com/reaction/1376631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoisobutyric acidHCID 6119—
ReactantTriethylamineHCID 8471—
ReactantEthyl trifluoroacetateHCID 9794—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Thiazol-2-ylmethanamineHCID 2756507—
ProductHCID 22916684HCID 2291668496.6%

Reaction Steps

To 2.5 g (0.024m mole) of 2-amino-2-methylpropanoic acid was added under ice-cooling 17 ml (0.122 mole) of triethylamine, followed by 15 ml (0.14 mole) of ethyl trifluoroacetate, and the mixture was stirred for 1 hour. Six milliliter (0.05 mole) of ethyl trifluoroacetate was added, and the mixture was further stirred for 20 hours. The reaction mixture was concentrated to dryness under reduced pressure. To the solution of the residue thus obtained in methylene chloride (20 ml) was added 5 g (0.036 mole) of 1-hydroxybenzotriazole at a temperature of 3° C., followed by 38 ml (0.036 mole) of 1.0M dicyclohexylcarbodiimide and 2.85 g (0.025 mole) of 2-aminomethylthiazole. The mixture was treated in the same manner as in Preparation 16 (a) to give 4.9 g of the title compound. Yield 66%. NMR (CDCl3) δ: 1.71 (6H, s), 4.80 (2H, d, J=5.6 Hz), 7.03 (1H, brs), 7.33 (1H, d, J=3.3 Hz), 7.72 (1H, d, J=3.3 Hz), 7.81 (1H, brs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663162
Source datasetuspto-grants-1997_09
ORD IDord-a851ce9be1a243af88a29265650b898d
Source noteuspto-grants-1997_09